Linked Data
ClinVar Variation Id:
464761
ClinVar RCV Id:
RCV000546943
dbSNP Id:
rs1555152548
gnomAD v4:
12-51913351-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.51913351G>T , CM000674.2:g.51913351G>T | GRCh38 |
| NC_000012.11:g.52307135G>T , CM000674.1:g.52307135G>T | GRCh37 |
| NC_000012.10:g.50593402G>T | NCBI36 |
| NG_009549.1:g.10934G>T , LRG_543:g.10934G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000547400.6:c.355+1G>T | ENSP00000446724.2:n.355+1G>T | |
| ENST00000551576.6:c.313+1G>T | ENSP00000455848.2:n.313+1G>T | |
| ENST00000552678.2:c.313+1G>T | ENSP00000457394.2:n.313+1G>T | |
| ENST00000388922.9:c.313+1G>T MANE Select | ENSP00000373574.4:n.313+1G>T | |
| ENST00000388922.8:c.313+1G>T | ENSP00000373574.4:n.313+1G>T | |
| ENST00000419526.6:c.103+816G>T | ENSP00000392492.2:n.103+816G>T | |
| ENST00000547400.5:c.355+1G>T | ENSP00000446724.1:n.355+1G>T | |
| ENST00000550683.5:c.355+1G>T | ENSP00000447884.1:n.355+1G>T | |
| NM_000020.2:c.313+1G>T , LRG_543t1:c.313+1G>T | NP_000011.2:n.313+1G>T | |
| NM_001077401.1:c.313+1G>T | NP_001070869.1:n.313+1G>T | |
| XM_005269235.2:c.313+1G>T | XP_005269292.1:n.313+1G>T | |
| XM_011539008.1:c.355+1G>T | XP_011537310.1:n.355+1G>T | |
| XM_024449279.1:c.-377+1G>T | XP_024305047.1:n.-377+1G>T | |
| NM_000020.3:c.313+1G>T MANE Select | NP_000011.2:n.313+1G>T | |
| NM_001077401.2:c.313+1G>T | NP_001070869.1:n.313+1G>T |